FINEPOINT LABS

Analytical Lab Programs for Regulated Science

A Health Canada–licensed (DEL · CDS), cGMP-compliant lab with Level 7 secure vault storage, built for pharmaceutical and controlled-substance work.

Potency Testing

Precise quantification of active pharmaceutical ingredients (APIs), cannabinoids, and controlled substances using validated HPLC, GC, and LC-MS/MS methodologies. Our Health Canada–licensed lab delivers defensible results, with detection limits suited to demanding matrices.

We specialize in complex matrices including botanicals, edibles, concentrates, and pharmaceutical formulations. Our potency analysis includes full cannabinoid profiles, terpene quantification, and impurity screening to meet your regulatory requirements.

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Key Features

  • HPLC, GC-MS, and LC-MS/MS validation
  • Full cannabinoid and terpene profiling
  • USP/ICH-aligned methodologies
  • 24–48 hour rush turnaround available

Safety & Compliance

Targeted safety panels for pesticides, heavy metals, mycotoxins, and residual solvents, supporting regulatory compliance for pharmaceutical, cannabis, and related products.

We operate under Health Canada licences (DEL · CDS) to cGMP standards and use only validated methods. Our safety testing includes over 60 pesticides, 20 heavy metals, and complete mycotoxin screening to protect consumer health and ensure market access.

Ensure Compliance

Comprehensive Coverage

  • 60+ pesticide residue analysis
  • Heavy metals and trace elements
  • Mycotoxins and microbial toxins
  • Residual solvents screening

Stability Studies

Long-term and accelerated stability testing to determine shelf-life, degradation kinetics, and storage recommendations per ICH guidelines. We design custom stability programs for pharmaceuticals and cannabis products.

Our stability chambers maintain precise temperature and humidity conditions, and we track degradation products, potency changes, and physical characteristics over time. Results support regulatory submissions and product labeling.

Start Stability Study

ICH-Aligned Programs

  • Long-term and accelerated studies
  • Degradation kinetics modeling
  • Custom storage conditions
  • Regulatory submission support

Microbial Testing

Comprehensive microbial contamination screening including total yeast/mold, E. coli, Salmonella, and pathogen identification. We use both traditional plating and advanced PCR methods for rapid results.

Our microbiology lab reports quantitative, interpretable results with action limits, tracking the organisms your product specification requires, with documentation matched to your safety requirements.

Test for Pathogens

Complete Microbial Analysis

  • Total aerobic microbial count
  • Yeast and mold quantification
  • Pathogen screening (E. coli, Salmonella)
  • 24–48 hour rush results available

Method Validation

Custom analytical method development and validation services designed to meet FDA, USP, and ICH guidelines for your specific matrix. We build robust methods from scratch or optimize existing procedures.

Our validation packages include full method characterization, system suitability testing, and documentation for regulatory submission. We work with pharmaceuticals, botanicals, and novel compounds.

Validate Your Method

Validation Parameters

  • Accuracy and precision testing
  • Linearity and range determination
  • Specificity and selectivity
  • LOD/LOQ establishment

Custom Solutions

Tailored analytical programs designed to address unique regulatory, research, or quality control challenges specific to your operation. We develop custom testing protocols for novel compounds and matrices.

Our scientific team works with you to clarify objectives, choose methods, and build a program that scales with your product, your regulatory file, or your production cadence.

Discuss Your Project

Bespoke Services

  • Novel compound analysis
  • Custom method development
  • Research-grade testing
  • Consulting and protocol design

Our Service Commitments

Analytical Precision

Advanced instrumentation, validated methods, and scientific review behind precise, defensible results.

Complete Coverage

From potency analysis to microbial screening, programs cover the key analytical requirements of a regulated product.

Regulatory Compliance

Documentation, validation, and practices aligned with Health Canada, USP, ICH, and the expectations of your target markets.

Innovation in Testing

Analytical approaches and custom protocols that advance your research, development, and product quality.

Need lab results you can defend?

Tell us the matrix, the compound, and the deadline. Rush 24–48h turnaround is available when the timeline is tight.

Contact Finepoint Labs